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Nasopharyngeal Epstein-Barr Virus Load: An Efficient Supplementary Method for Population-Based Nasopharyngeal Carcinoma Screening
被引:39
|作者:
Chen, Yufeng
[1
,2
,3
]
Zhao, Weilin
[1
,6
]
Lin, Longde
[2
,3
]
Xiao, Xue
[1
]
Zhou, Xiaoying
[1
]
Ming, Huixin
[1
]
Huang, Tingting
[1
,2
]
Liao, Jian
[4
]
Li, Yancheng
[4
]
Zeng, Xiaoyun
[2
,3
]
Huang, Guangwu
[1
,2
]
Ye, Weimin
[5
]
Zhang, Zhe
[1
,2
]
机构:
[1] Guangxi Med Univ, Affiliated Hosp 1, Dept Otolaryngol Head & Neck Surg, Nanning, Guangxi, Peoples R China
[2] Guangxi Med Univ, Minist Educ, Key Lab High Incidence Tumor Prevent & Treatment, Nanning, Guangxi, Peoples R China
[3] Guangxi Med Univ, Sch Publ Hlth, Dept Epidemiol, Nanning, Guangxi, Peoples R China
[4] Canc Inst Cangwu Cty, Wuzhou, Guangxi, Peoples R China
[5] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[6] Mie Univ, Grad Sch Med, Dept Environm & Mol Med, Tsu, Mie, Japan
来源:
PLOS ONE
|
2015年
/
10卷
/
07期
关键词:
DNA LOAD;
PLASMA;
EBV;
BRUSHINGS;
INFECTION;
DIAGNOSIS;
BLOOD;
GENE;
D O I:
10.1371/journal.pone.0132669
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Serological detection of Epstein-Barr virus (EBV) antibodies is frequently used in nasopharyngeal carcinoma (NPC) mass screening. However, the large number of seropositive subjects who require close follow-up is still a big burden. The present study aimed to detect the nasopharyngeal EBV load in a high-risk population seropositive for antibodies against EBV, as well as to examine whether assay for nasopharyngeal EBV DNA load might reduce the number of high-risk subjects for follow-up and improve early detection of NPC. A prospective and population-based cohort study was conducted in southern China from 2006 through 2013. Among 22,186 participants, 1045 subjects with serum immunoglobulin A (IgA) antibodies against viral capsid antigen (VCA) titers >= 1: 5 were defined as high-risk group, and were then followed-up for NPC occurrence. Qualified nasopharyngeal swab specimens were available from 905 participants and used for quantitative PCR assay. Our study revealed that 89% (802/905) subjects showed positive EBV DNA in nasopharyngeal swab. The nasopharyngeal EBV load in females was higher than that in males. The nasopharyngeal EBV load increased with increasing serum VCA/IgA titers. Eight cases of newly diagnosed NPC showed an extremely elevated EBV load, and 87.5% (7 of 8 patients) were early-stage NPCs. The EBV loads of 8 NPCs were significantly higher than those of 897 NPC-free subjects (mean, 2.8x10(6) copies/swab [range 4.8x10(4)-1.1x10(8)] vs. 5.6x10(3) [range 0-3.8x10(6)]). Using mean EBV load in NPC-free population plus two standard deviations as cut-off value, a higher diagnostic performance was obtained for EBV load test than serum VCA/IgA test (area under ROC, 0.980 vs 0.895). In conclusion, in a prospective and population-based study we demonstrated that an additional assay of EBV load in the nasopharynx among high-risk individuals may reduce the number of subjects needed to be closely followed up and could serve as part of a NPC screening program in high-risk populations.
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